A novel variant of the medicinally relevant 1,2,5-benzothiadiazepin-4-one-1,1-dioxide scaffold accessed via the downstream modification of Castagnoli-Cushman lactams
Author:
Funder
Russian Science Foundation
Saint Petersburg State University
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Recent Advances in the Development and Applications of Post-Ugi Transformations
2. Novel approach to the synthesis of nitrogen analogs of the tetrahydrocannabinols
3. New Heterocyclic Product Space for the Castagnoli–Cushman Three-Component Reaction
4. Bicyclic Piperazine Mimetics of the Peptide β-Turn Assembled via the Castagnoli–Cushman Reaction
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1. The Castagnoli–Cushman Reaction;Molecules;2023-03-15
2. Seven-Membered Rings With Three Heteroatoms 1,2,5;Comprehensive Heterocyclic Chemistry IV;2022
3. Efficient synthesis of seven-membered Aza-sultams: Heterofused amino-1,2,4-thiadiazepine dioxides;Tetrahedron;2021-05
4. Palladium(0)-catalysed regioselective cyclisations of 2-amino(tosyl) benzamides/sulphonamides: the stereoselective synthesis of 3-ylidene-[1,4]benzodiazepin-5-ones/benzo[f][1,2,5]thiadiazepine-1,1-dioxides;Chemical Communications;2021
5. Seven-membered rings;Progress in Heterocyclic Chemistry;2021
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